A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889447



Internal ID22664464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159567850..159567905hg38UCSC Ensembl
chr6:159988882..159988937hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889447
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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